Active Ingredient
Allantoin 0.5%
Benzethonium Chloride 0.5%
Terrasil Wound Care
FDA Label NDC 24909-115
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Aidance Skincare & Topical Solutions, Llc for the product Terrasil Wound Care (NDC 24909-115). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredient, purpose, uses, warnings, keep out of reach of children., directions, inactive ingredients, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Allantoin - Skin Protectant
Benzethonium Chloride - Antiseptic
Uses
Temporarily protects minor cuts, scrapes, burns. Helps relieve chapped or cracked skin and lips. Helps protect from the drying effects of wind and cold weather. First aid to help decrease the risk of skin infection.
Warnings
For external use only. When using this product, do not get into eyes. Stop use and ask a doctor if condition worsens, symptoms last more than 7 days or clear up and occur again within a few days. Do not use on deep or puncture wounds, animal bites or serious burns.
Keep Out Of Reach Of Children.
If swallowed, call poison control or seek medical help.
Directions
Wash and dry affected skin. Apply a thin layer of Terrasil. Cover affected area with a clean bandage. Repeat procedure 2-3 times daily until skin improves. Store at room temperature.
Inactive Ingredients
(Organic) Beeswax, Bentonite, Simmondsia Chinensis (Jojoba) Seed Oil, Magnesium Oxide, Peppermint Oil, Sage Oil, Silver Oxide,
Zinc Oxide
Package Label.Principal Display Panel
Jar Label (Terrasil Wc Label 01192012)
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